ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.1528T>C (p.Tyr510His)

dbSNP: rs201404055
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000593003 SCV000704928 uncertain significance not provided 2017-01-20 criteria provided, single submitter clinical testing
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001261086 SCV001438488 uncertain significance Noonan syndrome no assertion criteria provided clinical testing

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